DRAP REGISTERED MEDICAL DEVICE
Wondfo 2019-nCoV Antigen Test Device (Lateral Flow Method) [W196] is registered with DRAP under number MDIR-0002579 as a Class C (moderate to high risk) medical device, imported. The listed holder is Schazoo SPL Consumer Healthcare. Its listed renewal date (3 Jun 2026) has passed, so ask the supplier for the renewal letter.
Screening result
MDIR-0002579 · the class is taken from DRAP's list for this number
DRAP registered Class B/C/D list, 28 Aug 2025
It may have been renewed after DRAP's last list. Ask the vendor for the renewal letter.
ELI-00095
| Device | Wondfo 2019-nCoV Antigen Test Device (Lateral Flow Method) [W196] |
|---|---|
| Class | C |
| Listed holder | Schazoo SPL Consumer Healthcare |
| Holder address | 71-B/C2, Gulberg-III, Lahore |
| Manufacturing site | M/s Guangzhou Wondfo Biotech Co., Ltd., No. 8 Lizhishan Road, Science City, Luogang District, 510663, Guangzhou, China |
| Issued | 4 Jun 2021 |
| Renewal date | 3 Jun 2026 |
| Licence | ELI-00095 |
Specifications
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Screened 5 Oct 2026, 21:58 (Pakistan time). A screening aid, not an official DRAP verification.
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Corrections
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Source: DRAP's published provisional lists. A screening aid, not an official DRAP verification; confirm with DRAP and the supplier's original documents.